Functional Service Provider (FSP) Solutions

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THE VED CONSULTING

Functional Service Provider (FSP) Solutions

Comprehensive Support for Clinical Trials

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Welcome to the ved consulting

OVERVIEW

The VED Consulting’s FSP Solutions offer a full range of services to support every phase of your clinical trials. From feasibility assessment to study completion, we provide tailored solutions that enhance trial effectiveness and patient centricity. With deep therapeutic expertise across a wide range of indications, including oncology, rare diseases, and dermatology, we deliver high-quality solutions for all types of clinical research engagements.

Key regions Talent resourcing

Talent resourcing services for the key regions of North America, Europe, and India

Extensive Network

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Best Talent

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Launch

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How we work

Why choose The Ved Consulting

Global Feasibility

Conducting comprehensive feasibility assessments to identify potential challenges and ensure the viability of your clinical trials.

Site Identification & Selection

Identifying and selecting the most suitable sites globally, maximizing recruitment potential.

Global Study Startup

Streamlining study startup processes, including site activation, regulatory document collection, and contract negotiation.

Patient & Site Engagement:

Implementing patient-centric strategies to enhance recruitment, retention, and site engagement.

eTMF & Document Management

Managing electronic Trial Master File (eTMF) systems, ensuring accurate and compliant document management.

Clinical Monitoring

Offering both on-site and remote monitoring to ensure trial integrity and data accuracy.

Hybrid & Decentralized Trial Solutions

Providing flexible trial solutions that combine traditional and decentralized approaches.

Biometrics

Delivering comprehensive biometric services, including statistical analysis, data management, and bioinformatics.

Medical Monitoring

Ensuring patient safety and data integrity through continuous medical oversight.

Safety & Pharmacovigilance

Monitoring and reporting safety data, ensuring compliance with global regulatory standards.

Medical Writing

Developing high-quality clinical and regulatory documents, including protocols and clinical study reports.

Quality & Validation

Ensuring all processes and systems meet regulatory requirements through rigorous quality and validation procedures.

Supply Chain Management

Managing the logistics of clinical trial supplies, including drug distribution and inventory management.

Therapeutic Expertise

Leveraging deep therapeutic expertise in oncology, rare diseases, and dermatology to provide specialized support for your clinical trials.

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Like to Get Started?

Strengthen your FSP Solutions with our expert support. Contact The VED Consulting today to learn how we can assist with adverse event reporting and safety database management.

THE VED CONSULTING